Cargando...
Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children
INTRODUCTION: Hirschsprung disease (HSCR), characterized by the defective migration of enteric neural crest cells, is a severe congenital tract disease in infants. Its etiology is not clear at present, although a genetic component plays an important role in its etiology. Many studies focused on the...
Gardado en:
| Publicado en: | J Gene Med |
|---|---|
| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2021
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7900950/ https://ncbi.nlm.nih.gov/pubmed/33294994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jgm.3301 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|